ENST00000269980.7:c.732G>T
MANE Select
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ENSP00000269980.2:p.Gly244=
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ENST00000269980.6:c.732G>T
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ENSP00000269980.2:p.Gly244=
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ENST00000457836.6:c.666G>T
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ENSP00000416000.2:p.Gly222=
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ENST00000535632.5:n.361G>T
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ENST00000540732.3:c.834G>T
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ENSP00000443246.1:p.Gly278=
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ENST00000541315.1:c.632G>T
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ENST00000542943.5:c.645G>T
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ENSP00000440345.1:p.Gly215=
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ENST00000545787.1:n.360G>T
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ENST00000595085.5:c.732G>T
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ENSP00000471150.2:p.Gly244=
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NM_000709.3:c.732G>T
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NP_000700.1:p.Gly244=
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NM_001164783.1:c.732G>T
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NP_001158255.1:p.Gly244=
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NM_000709.4:c.732G>T
MANE Select
|
NP_000700.1:p.Gly244=
|
|
NM_001164783.2:c.732G>T
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NP_001158255.1:p.Gly244=
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